Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 25 of 25 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g47280 A02 38149469 C T upstream_gene_variant MODIFIER c.-4476C>T| S181
2 BAA02g47280 A02 38149854 G A upstream_gene_variant MODIFIER c.-4091G>A| S132
S137
S215
3 BAA02g47280 A02 38150484 C T upstream_gene_variant MODIFIER c.-3461C>T| S122
4 BAA02g47280 A02 38152062 C T upstream_gene_variant MODIFIER c.-1883C>T| S173
5 BAA02g47280 A02 38152161 G A upstream_gene_variant MODIFIER c.-1784G>A| S261
6 BAA02g47280 A02 38152930 G A upstream_gene_variant MODIFIER c.-1015G>A| S205
7 BAA02g47280 A02 38153149 G A upstream_gene_variant MODIFIER c.-796G>A| S44
8 BAA02g47280 A02 38153158 G A upstream_gene_variant MODIFIER c.-787G>A| S159
S243
9 BAA02g47280 A02 38153286 G A upstream_gene_variant MODIFIER c.-659G>A| S139
10 BAA02g47280 A02 38153722 C T upstream_gene_variant MODIFIER c.-223C>T| S180
11 BAA02g47280 A02 38155190 G A missense_variant MODERATE c.1246G>A|p.Gly416Ser S197
12 BAA02g47280 A02 38155217 C T missense_variant MODERATE c.1273C>T|p.Pro425Ser S77
S82
13 BAA02g47280 A02 38156217 C T synonymous_variant LOW c.1479C>T|p.Arg493Arg S182
14 BAA02g47280 A02 38157369 G A intron_variant MODIFIER c.1861+770G>A| S10
15 BAA02g47280 A02 38157549 C T intron_variant MODIFIER c.1862-773C>T| S188
16 BAA02g47280 A02 38157568 C T intron_variant MODIFIER c.1862-754C>T| S208
S93
17 BAA02g47280 A02 38157656 C T intron_variant MODIFIER c.1862-666C>T| S277
18 BAA02g47280 A02 38157723 G A intron_variant MODIFIER c.1862-599G>A| S288
19 BAA02g47280 A02 38158572 G A missense_variant MODERATE c.2112G>A|p.Met704Ile S259
20 BAA02g47280 A02 38158913 C T missense_variant MODERATE c.2453C>T|p.Thr818Ile S98
21 BAA02g47280 A02 38159315 G A missense_variant MODERATE c.2855G>A|p.Gly952Glu S298
22 BAA02g47280 A02 38163985 G A downstream_gene_variant MODIFIER c.*4396G>A| S71
23 BAA02g47280 A02 38164354 C T downstream_gene_variant MODIFIER c.*4765C>T| S260
24 BAA02g47280 A02 38164439 G A downstream_gene_variant MODIFIER c.*4850G>A| S13
25 BAA02g47280 A02 38164511 C T downstream_gene_variant MODIFIER c.*4922C>T| S9